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Environmental fate & pathways

Biodegradation in water: screening tests

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Reference
Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 310 (Ready Biodegradability - CO2 in Sealed Vessels (Headspace Test)
GLP compliance:
yes
Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, non-adapted
Details on inoculum:
- Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): Activated sludge was collected from the Cambridge Wastewater Treatment Facility, Cambridge, Maryland on March 30, 2009. The Cambridge facility treats predominantly residential wastes.

- Preparation of inoculum for exposure: The sludge was sieved using a 2-mm screen and then aerated at test temperature until its adjustment. The activated sludge was diluted in test medium to approximately 30 mg total suspended solids/L and aerated with CO2-free air until its adjustment. The inoculated medium used in the test was prepared by diluting the preconditioned activated sludge in test medium to 4 mg total suspended solids/L.
Duration of test (contact time):
28 d
Initial conc.:
20 mg/L
Based on:
DOC
Parameter followed for biodegradation estimation:
CO2 evolution
Details on study design:

TEST SYSTEM
- Culturing apparatus: glass serum bottles with a nominal volume of 160 mL. The chambers were sealed with butyl rubber septa and crimp caps.


SAMPLING
- Sampling frequency: Replicate chambers from the control, reference and treatment groups were removed for IC analysis once a week over the test period. Replicate chambers from the toxicity control group were removed for IC analysis on Days 1 and 28. Three replicate test chambers from each group were analyzed at each respective sacrifice interval, except for the last interval (5 replicates each).

- Sampling method: Samples for analysis were prepared by converting CO2 to carbonate. One milliliter of 7M NaOH was injected into the test chambers, which were subsequently shaken for at least 1 hour at test temperature. After mixing, the chambers were removed from the shaker table, allowed to settle and then samples were removed for IC analysis.
Reference substance:
benzoic acid, sodium salt
Parameter:
% degradation (CO2 evolution)
Value:
0
Sampling time:
28 d
Details on results:
Test substance: -3.7% in 28 days
Reference substance: 96.5% in 28d (>60% in 7 days)
Toxicity control: 46.2% in 28d

Table 1: Inorganic carbon concentration (mg C/l) and calculated % biodegradation for inoculum blank, reference substance, test substance and toxicity control

Type of suspension

1d

7d

14d

21d

28d

 

Inorg. C (mgC/l)

(%) biodeg

Inorg. C (mgC/l)

 (%) biodeg

Inorg. C (mgC/l)

(%) biodeg

Inorg. C (mgC/l)

(%) biodeg

Inorg. C (mgC/l)

(%) biodeg

Cumulative average (%) biodeg (Day 28)

 

 

 

 

 

 

 

 

 

 

Inoculum Blank

-

-

0.3; 0.1; 0.4

-

2.3; 2.4; 1.8

-

2.9; 2.8; 3.1

-

2.8; 2.8; 3.1; 2.6; 3.1

-

-

 

 

 

 

 

 

 

 

 

Reference substance

-

-

16.9; 16.8; 17.4

83.8; 83.4; 86.1

18.8; 19.5; 19.1

84.1; 87.4; 85.4

20.5; 20.4; 20.4

88.4; 88.2; 88.2

22.1; 22.0; 22.2; 21.9; 21.9

96.7; 96.3; 97.5; 96.1; 95.8

96.5

 

 

 

 

 

 

 

 

 

Test substance

-

-

0.1; 0.0; 0.0

-0.7; -1.3; -1.5

1.9; 2.3; 1.5

-1.5; 0.4; -3.2

2.4; 2.3; 2.4

-2.9; -3.2; -2.6

2.2; 2.2; 2.4; 2.1; 2.0

-3.5; -3.7; -2.6; -3.9; -4.6

-3.7

 

 

 

 

 

 

 

 

 

Toxicity control

13.4; 13.6; 13.6

33.7; 34.3; 34.4

-

-

-

-

-

-

21.3; 21.1; 21.1; 21.4; 20.9

46.6; 46.0; 45.9; 46.8; 45.5

46.2

 

 

 

 

 

 

 

 

 

 

Validity criteria fulfilled:
yes
Interpretation of results:
under test conditions no biodegradation observed
Conclusions:
0% biodegradation in 28 days was determined in a reliable study conducted according to an appropriate test protocol, and in compliance with GLP.

Description of key information

Biodegradation in water: screening tests: 0% in 28 days (OECD 310), read-across from a structurally-related substance.

Key value for chemical safety assessment

Biodegradation in water:
under test conditions no biodegradation observed

Additional information

There are no reliable ready biodegradation data available for tetradecamethylhexasiloxane (L6), therefore good quality data for the structurally-related substance, octamethyltrisiloxane (L3, CAS No. 107-51-7), have been read across. L6 and L3 are structurally-similar substances, both are linear siloxanes.

L3 is a linear siloxane chain with three silicon atoms, connected by two oxygen atoms. All silicon atoms present are fully substituted with methyl groups. L6 is a structurally related linear siloxane, with six silicon atoms and five oxygen atoms.

 

L3 and L6 are within a group of substances within which, in general, there is no evidence of any significant biodegradation.

The table below presents ready biodegradation data for substances within the group of siloxanes (alkyl, vinyl, aryl or hydrogen substituted).

It is therefore considered valid to read-across the results for L3 to fill the data gap for the registered substance. Additional information is given in a supporting report (PFA, 2017at) attached in Section 13.

Table 4.5: Ready biodegradation data for substances within the siloxane group

CAS

Name

Readily biodegradable? Yes/no

Result: Biodegradation after 28 days (%)*

Guideline

Test type

Reliability

107-46-0

Hexamethyldisiloxane

No

2%

OECD 301C

BOD

1

107-51-7

Octamethyltrisiloxane

No

-3.70%

OECD 310

CO2

1

540-97-6

Dodecamethylcyclohexasiloxane

No

4.5%

OECD 310

CO2

1

541-02-6

Decamethylcyclopentasiloxane

No

0.14%

OECD 310

CO2

1

541-05-9

Hexamethylcyclotrisiloxane

No

0.06%

OECD 310

CO2

1

556-67-2

Octamethylcyclotetrasiloxane

No

3.70%

OECD 310

CO2

1

1873-88-7

1,1,1,3,5,5,5-Heptamethyltrisiloxane

No

0%

OECD 310/ ISO Guideline No 14593

CO2

1

2627-95-4

1,1,3,3-Tetramethyl-1,3-divinyldisiloxane

No

0%

OECD 301D

BOD

1

17928-28-8

1,1,1,3,5,5,5-Heptamethyl- 3-[(trimethylsilyl)oxy] trisiloxane

No

0%

OECD 301F

BOD

1

17955-88-3

1,1,1,3,5,5,5-Heptamethyl-3-octyltrisiloxane

No

10 – 32 % after 25 d

OECD 301B

CO2

 1

60111-47-9

3-[(Dimethylvinylsilyl)oxy]-1,1,5,5-tetramethyl-3-phenyl-1,5-divinyltrisiloxane

No

2.20%

OECD 301F

BOD

1

69304-37-6

1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane

No

0% (BOD); 100% (GC)

OECD 301C

BOD

1

70940-00-0

1,1,7,7,-Tetramethyl-3,3,5,5,-Tetraphenyl-Tetrasiloxane

No

9.7 and 9.9%

OECD 301B

CO2

 1

180073-46-5

Pentasiloxane, 1,1,9,9-tetramethyl-3,3,5,5,7,7-hexaphenyl-

No

5.2 and 4.4%

OECD 301B

CO2

 1

352230-22-9

Siloxanes and Silicones, di-Ph, Ph (trimethylsilyl)oxy

No

0%

OECD 301F

BOD

1

In the study with L3, 0% biodegradation was observed in 28 days.

The study was conducted according to OECD 310 and is considered reliable. This is selected as the key study.

References: PFA. (2017at): Siloxane Category Report for Environmental Endpoints. Owner company: Reconsile. Report date: 2017-06-02